Open Access

Evaluation of the anticancer potential of six herbs against a hepatoma cell line

  • Natthida Weerapreeyakul1, 2Email author,
  • Apiyada Nonpunya3,
  • Sahapat Barusrux2, 4, 5,
  • Thaweesak Thitimetharoch1, 2 and
  • Bungorn Sripanidkulchai1, 2
Chinese Medicine20127:15

DOI: 10.1186/1749-8546-7-15

Received: 5 January 2012

Accepted: 1 June 2012

Published: 10 June 2012



Six herbs in the Plant Genetics Conservation Project that have been used as complementary medicines were chosen on the basis of their medicinal value, namely Terminalia mucronata, Diospyros winitii, Bridelia insulana, Artabotrys harmandii, Terminallia triptera, and Croton oblongifolius. This study aims to evaluate the potential anticancer activity of 50% ethanol-water extracts of these six herbs.


Fifty percent ethanol-water crude extracts of the six herbs were prepared. The cytotoxicity of the herbal extracts relative to that of melphalan was evaluated using a hepatoma cell line (HepG2), and examined by neutral red assays and apoptosis induction by gel electrophoresis and flow cytometry after 24 h.


A significant difference was found between the cytotoxicity of the 50% ethanol-water crude extracts and melphalan (P = 0.000). The 50% ethanol-water crude extracts of all six herbs exhibited cytotoxicity against HepG2 cells, with IC50 values ranging from 100 to 500 μg/mL. The extract of T. triptera showed the highest cytotoxicity with an IC50 of 148.7 ± 12.3 μg/mL, while melphalan had an IC50 of 39.79 ± 7.62 μg/mL. The 50% ethanol-water crude extracts of D. winitii and T. triptera, but not A. harmandii, produced a DNA ladder. The 50% ethanol-water crude extracts of D. winitii, T. triptera, and A. harmandii induced apoptosis detected by flow cytometry.


The 50% ethanol-water crude extracts of D. winitii, T. triptera, and A. harmandii showed anticancer activity in vitro.


The Plant Genetics Conservation Project, under the patronage of Her Royal Highness Princess Maha Chakri Sirindhorn, aims to evaluate the biochemical activities and properties of potential medicinal plants. Previously, cytotoxic and apoptotic effects of medicinal plants found in Chaiyaphum province have been discovered[1]. Therefore, subsequent studies were extended for herbs in other Plant Genetics Conservation Project areas, including Terminalia triptera Stapf and Terminalia mucronata Craib & Hutch in Combretaceae, Croton oblongifolius Roxb. and Bridelia ovata Decne in Euphorbiaceae, Diospyros winitii Fletcher in Ebenaceae, and Artabotrys harmandii Finet & Gagnep. in Annonaceae. Except for T. mucronata and A. harmandii, the other four herbs are all found in China[2, 3].

The abovementioned herbs are commonly used in Asia[2, 3]. For example, the bark of T. triptera is used with betel nuts as a remedy for aphthous ulcer[3]. Meanwhile, for C. oblongifolius, its leaves are used as a tonic for indigestion, flatulence, and bruises, its flowers for the treatment of flat worms, its fruit for dysmenorrhea, its seeds as a purgative, its roots for dysentery, and its bark for dyspepsia, chronic hepatomegaly, and fever[3]. The medicinal use of D. winitii is unclear. The longstanding medicinal use of these herbs necessitates research into their clinical safety and rigorous biological activity testing. Since cancer is a leading cause of death worldwide[4], evaluation of the anticancer activity of these herbs is the first priority. It was previously reported that labdane diterpenoids extracted from the stem bark of C. oblongifolius exert moderate cytotoxicity toward cancer cell lines[5].

In this study, determination of anticancer activity was based on the cytotoxicity of 50% ethanol-water crude extracts toward a human hepatocarcinoma cell line, HepG2. Cytotoxicity and selectivity were determined for the safety of the 50% ethanol-water crude extracts using a normal African green monkey kidney epithelial cell line, Vero, relative to the HepG2 cell line. Apoptotic cell death is a protective mechanism that destroys misprogrammed or nonfunctional cells and is used as a clinical endpoint for effective anticancer treatment[6, 7]. The apoptosis-inducing effects were determined in HepG2 cells by examination of DNA fragmentation, which is observed as DNA laddering by agarose gel electrophoresis. The apoptosis-inducing effects of the plant extracts were further confirmed using Annexin V-FITC staining and detection by flow cytometry.

In this study, we aims to investigate the anticancer activity of six herbs based on their cytotoxicity and apoptosis induction.


Chemicals and reagents

Dulbecco’s modified Eagle’s medium (DMEM), fetal bovine serum (FBS), penicillin, and streptomycin were purchased from GIBCO® (Invitrogen, USA). Dimethylsulfoxide (DMSO) and ethidium bromide were purchased from Sigma-Aldrich (USA). Sodium bicarbonate, neutral red (NR), and melphalan in powder form were purchased from Sigma-Aldrich (Germany). Isopropyl alcohol (biotechnology grade) was purchased from Bio Basic Inc. (USA). Methanol (analytical grade) was purchased from BDH (England). A FlexiGene DNA Kit was obtained from Qiagen (Germany). Agarose (molecular grade) was purchased from Bio-Rad (USA), and an 100 bp + 1.5 Kb DNA ladder with stain was purchased from SibEnzyme (Russia). All other reagents used in this study were purchased from Sigma Chemicals Co. (USA). An Annexin V-FITC Apoptosis Detection Kit was purchased from Bender MedSystems GmbH (Austria).

Herb materials

Twigs of the six herbs were collected and authenticated by Assistant Professor Thaweesak Thitimetharoch based on the taxonomy [TT, OC & SK-number]. The vouchers were deposited at the Herbal Herbarium, Faculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen Province, Thailand. The details of the herbs and voucher numbers are summarized in Table1.
Table 1

Cytotoxicity of the 50% ethanol-water crude extracts based on the neutral red assay, and the scientific name, family, part used and % yield

Scientific name (Voucher specimen no.)


% yield per gram dry weight

Cytotoxicity (IC50 value, μg/mL)

T. triptera



136.4 ± 44.5

148.7 ± 12.3

[TT, OC & SK No 1214, 1224]

C. oblongifolius



238.9 ± 21.9

378.4 ± 18.7

[TT, OC & SK No 1215, 1256]

D. winitii



> 500

204.7 ± 33.5

[TT, OC & SK No 1245]

B. ovata



> 500

183.9 ± 7.1

[TT, OC & SK No 1253]

A. harmandii



309.7 ± 58.2

163.5 ± 11.7

[TT, OC & SK No 1264]

T. mucronata



129.4 ± 18.4

152.0 ± 33.2

[TT, OC & SK No 1269]



59.9 ± 3.2

37.7 ± 9.8

Herb extractions

Fifty percent ethanol-water crude extracts were prepared from the dried stems of each herb, which were cut and macerated with 50% ethanol-water at a ratio of 1 kg/6 L for 7 days with occasional shaking. The solvent was filtered, distilled in vacuo using a rotary evaporator (Rotavapor R-200; Büchi Labortechnik AG, Switzerland) below 40°C, and freeze-dried to obtain the 50% ethanol-water crude extracts. The 50% ethanol-water extracts were freshly prepared as stock solutions in DMSO.

Gas chromatography/mass spectrometry (GC-MS) analysis

A gas chromatography system (Model 6890 N; Agilent Technologies, China) coupled with a mass selective detector (Model 5973 N; Agilent Technologies, USA) and a GC autosampler (HP 7683 series) were employed for all analyses. Samples were separated on a 30.0-m long, 250-μm diameter, 0.25-μm film thickness, 122–5532 DB-5 ms capillary column from Agilent Technologies (J&W Scientific, USA). The column initially flowed at 80°C for 6 min with a rate of 2 mL/min and an average velocity of 52 cm/s. The temperature was then raised to 280°C (at a rate of 5°C/min) and maintained for 24 min. The total runtime was 70 min. Ultrapure helium with an inline Alltech oxygen trap was used as the carrier gas (19.34 psi), with the purge flow set at 20.0 mL/min, the purge time set at 0.75 min, and a total flow of 24.3 mL/min. The injector temperature was maintained at 250°C, and the injection volume at 2.0 μL in the splitless mode. The interface temperature was held at 280°C. Mass spectra were scanned from m/z 50.0 to m/z 500.0 at a rate of 1.5 scans/s with a threshold of 150. The electron impact ionization energy was 70 eV. The chemical components of the crude extracts were identified from the chromatograms and mass spectra using the Wiley 7 N.l database (Agilent Technologies).

Cell culture

The HepG2 and Vero cell lines were maintained at the Center for Research and Development of the Medical Diagnostic Laboratories, Khon Kaen University. DMEM was supplemented with 10% FBS, 100 U/mL penicillin, and 100 μg/mL streptomycin. The cells were cultured at 37°C under a humidified atmosphere containing 5% CO2.

Cytotoxicity based on NR assays

The stock solutions of the herb extracts in DMSO were diluted with DMEM to the desired concentrations (10–500 μg/mL). The maximum concentration of the 50% ethanol-water extracts in each test was 500 μg/mL, such that the final concentration of DMSO would not exceed 1% (v/v) and the cytotoxicity of DMSO would be less than 10%. The HepG2 hepatoma cell line and normal Vero cell line were used as the cell models. The cytotoxicity evaluation was performed using NR assays according to Fotakis and Timbrell[8], with some modifications. Melphalan was used as a standard anticancer drug for comparisons with the crude extracts.

The cells were seeded in 96-well plates at a density of 3 × 105 cells/mL and treated with different concentrations of the 50% ethanol-water crude extracts or melphalan for 24 h. The cells were then washed and the supernatants were discarded. The NR was dissolved in 100 μL of 0.33% HCl. The NR solution was added to each well, yielding a final concentration of 50 μg/mL, and incubated at 37°C for 1 h. The absorbance of the NR dye was detected using a dual-wavelength UV spectrometer (Anthos 2010; Biochrom, UK) at 520 nm with a reference wavelength of 650 nm. The percent cytotoxicity compared with untreated cells was determined and calculated as the %-cytotoxicity. A plot of %-cytotoxicity vs. test compound concentration was used to calculate the IC50. The selectivity index (SI) was calculated from the IC50 of the 50% ethanol-water crude extracts in normal cells vs. cancer cells to indicate the cytotoxic selectivity (i.e., safety) of the 50% ethanol-water crude extracts against cancer cells vs. normal cells.

Apoptosis induction assays

DNA fragmentation detection assay

DNA fragmentation was used as a proxy for apoptosis induction. After treatment of cancer cells with 500 μg/mL of the 50% ethanol-water extracts and 80 μg/mL of melphalan for 24 h, the cells were collected and washed with medium. The cell suspensions were transferred to microcentrifuge tubes (1.5 mL) and centrifuged at 500 × g (PMI-Labortechnik GmbH, Germany) for 5 min, followed by collection of the cell pellets. The DNA in the cell pellets was extracted using a FlexiGene DNA Kit according to the web-published FlexiGene® DNA Handbook. Aliquots (2 μg) of the DNA were analyzed by electrophoresis in 1.8% agarose gels containing 0.1% ethidium bromide. After the electrophoresis, the DNA fragments were analyzed using a UV-illuminated camera (Syngene, UK).

Annexin V-FITC staining for apoptosis detection by flow cytometry

An Annexin V-FITC and propidium iodide (PI) double staining method was used according to Moosavi and Yazdanparast[9], with some modifications. The cells were seeded in a 24-well plate at a density of 5 × 105 cells/mL, supplemented with DMEM containing 10% FBS, and incubated in a 5% CO2 incubator at 37°C for 24 h. The test compounds were added to the wells to give final concentrations of 500 μg/mL for the respective 50% ethanol-water extracts and 80 μg/mL for melphalan. The exposure time between the cells and the test compounds was 24 h. Subsequently, the cells were washed with 1 × phosphate-buffered saline (PBS), trypsinized, and transferred to microcentrifuge tubes (1.5 mL). The cells were centrifuged at 500 × g, and the cell pellets were resuspended with 195 μL of binding buffer (10 mM HEPES/NaOH pH 7.4, 140 mM NaCl, 2.5 mM CaCl2). The cells were then stained with 5 μL of Annexin V-FITC in the dark at room temperature for 5 min and centrifuged at 500 × g to collect the cell pellets. Next, the cell pellets were resuspended in 190 μL of binding buffer and stained with 10 μL of PI for 10 min under the same conditions. Finally, the fluorescence intensity was determined using a flow cytometer (FACSCanto II; BD Biosciences, USA), and the percentages of cells in different populations were quantified using a quadrant marker.

Statistical analysis

The data were represented as means ± standard deviation (SD) (n = 3). The statistical significance of differences in multiple-group comparisons were evaluated by a one-way analysis of variance followed by Tukey’s Honestly Significant Difference test using SPSS version 11.5 (SPSS Inc., USA). A two-tailed Student’s t-test was also performed. Values of P < 0.05 were considered statistically significant within a 95% confidence interval.

Results and discussion

The 50% ethanol-water crude extracts of the six herbs showed moderate cytotoxicity toward HepG2 and Vero cells, except for the lack of activity of the D. winitii and B. ovata extracts toward Vero cells (IC50 > 500μg/mL).

The 50% ethanol-water crude extracts of the six herbs exhibited different degrees of cytotoxicity toward HepG2 cells, with IC50 values ranging from 100 to 500 μg/mL, and showed significant differences from untreated cells (P = 0.000). The T. triptera extract showed high cytotoxicity toward HepG2 cells (IC50 = 148.7 ± 12.3 μg/mL). A significant difference was found between the cytotoxicity of melphalan and the 50% ethanol-water crude extracts (P = 0.000). All of the 50% ethanol-water crude extracts showed significantly lower cytotoxicity than melphalan (IC50 = 37.7 ± 9.8 μg/mL) (P = 0.000).

T. triptera and T. mucronata, which are both in the genus Terminalia of the family Combretaceae, were the most cytotoxic herbs toward HepG2 cells. In HepG2 cells, no significant differences in cytotoxicity were observed between T. triptera and T. mucronata (P = 1.000), T. triptera and A. harmandii (P = 0.862), D. winitii and B. ovate (P = 1.000), D. winitii and A. harmandii (P = 0.419), B. ovata and A. harmandii (P = 0.385), and T. mucronata and A. harmandii (P = 0.862). For Vero cells, no significant differences in cytotoxicity were observed between D. winitii and B. ovata (P = 1.000) and T. triptera and T. mucronata (P = 0.999).

The cytotoxicity and SI values of the plant extracts for HepG2 cells vs. Vero cells are summarized in Table2. The extracts showing significant differences in cytotoxicity (Student’s t-test) toward HepG2 cells compared with normal Vero cells similar to that of melphalan (P = 0.000) were C. oblongifolius (P = 0.002), D. winitii, (P = 0.000), B. ovata (P = 0.000), and A. harmandii (P = 0.005). None of the extracts had an SI value of > 3 for classification as highly selective.
Table 2

Classification of the cytotoxicity and selectivity index (SI) of the 50% ethanol-water crude extracts in HepG2 cells vs. Vero cells


SI Value

HepG2 vs. Vero

Very strong cytotoxicity

SI ≥ 3


(IC50 < 10 μg/mL)

Strong cytotoxicity

SI ≥ 3


(IC50 10 - 100 μg/mL)

SI < 3


Moderate cytotoxicity

SI ≥ 3


(IC50 100 - 500 μg/mL)

SI < 3


B. ovata (> 2.72)

D. winitii (> 2.44)

A. harmandii (1.89)

T. triptera (0.92)

T. mucronata (0.85)

C. oblongifolius (0.63)

The 50% ethanol-water extracts had only moderate anticancer activity, as evaluated by apoptosis induction. The distinct DNA ladder in HepG2 cells showed the characteristics of late-stage apoptosis after treatment with melphalan for 24 h (Figure1). The extracts of D. winitii and T. triptera showed subtle DNA ladders, while the other extracts did not induce the late-stage of apoptosis in HepG2 cells
Figure 1

DNA laddering in apoptotic HepG2 cells. DNA laddering was visualized in HepG2 cells after treatment with 80 μg/mL of melphalan and 500 μg/mL of 50% ethanol-water crude extracts for 24 h.

However, the DNA ladder assay has lower sensitivity for apoptosis detection than flow cytometry[10], because DNA ladder formation can only be clearly observed when the extent of oligonucleosomal cleavage is remarkable. Moreover, necrotic cells can also generate DNA fragments[11]. Therefore, the apoptosis findings obtained by Annexin V/PI staining, as detected by flow cytometry, may provide more details.

Percent cell populations at different death modes detected by Annexin V-FITC staining and flow cytometry after HepG2 cells treated with melphalan and 50% ethanol-water extracts for 24 h were shown in Figure2. Results show that four extracts induced apoptosis vs. untreated HepG2 cells at the late stage, with the most effective being A. harmandii, T. triptera, D. winitii, and C. oblongifolius. Melphalan induced 10.1% early-stage apoptosis and 6.2% late-stage apoptosis, and also caused 13.5% necrosis. Melphalan induced a significantly different %-apoptosis than the plant extracts (P = 0.000). Moreover, significant differences in the mean %-apoptosis were observed between D. winitii and A. harmandii (P = 0.000), T triptera and A. harmandii (P = 0.000), T. mucronata and A. harmandii (P = 0.000), C. oblongifolius and A. harmandii (P = 0.000), and A. harmandii and B. ovata (P = 0.000). Among the six herbs, the A. harmandii extract induced the highest degree of apoptosis by causing 2.1% early-stage apoptosis and 44.7% late-stage apoptosis with 32.6% high necrosis in HepG2 cells.
Figure 2

Percent cell populations at different death modes and percent viable cells detected by Annexin V-FITC staining and flow cytometry after treatment of HepG2 cells with 80 μg/mL of melphalan and 500 μg/mL of 50% ethanol-water crude extracts for 24 h. A: Untreated cells; B: melphalan-treated cells; C: Diospyros winitii-treated cells; D: Terminalia triptera-treated cells; E: Terminalia mucronata-treated cells; F: Croton oblongifolius-treated cells; G: Artabotrys harmandii-treated cells; H: Bridelia ovata-treated cells.

B. ovata, D. winitii, and A. harmandii were potentially cytotoxic with relatively high selectivity for HepG2 cells. Only A. harmandii showed high apoptosis in HepG2 cells (especially late-stage apoptosis) and a relatively high necrosis effect. B. ovata and D. winitii induced relatively higher necrosis in HepG2 cells than apoptosis, based on Annexin V/PI staining. These data suggested that the cell death among HepG2 cells induced by these two herbs was mostly necrosis. Since necrosis is an irreversible inflammatory form of cell death, it has some implications for cancer therapy[12]. Thus, B. ovata and D. winitii may be of interest for further investigations into their anticancer activity via necrosis as the mode of death.

Since 50% ethanol-water crude extracts were used in the present study, standardization of the three potential crude extracts for future quality control experiments was necessary. We then determined whether the phytochemicals in the crude extracts were associated with the apoptosis effects. GC-MS analyses of the D. winitii, T. triptera, and A. harmandii extracts were conducted. The GC peaks obtained were used for further chemical constituent identification using the MS database. The GC-MS analyses of the three crude extracts are shown in Additional files1,2, and3 and the main chemical constituents are presented in Table3.
Table 3

GC-MS profiles of the three potential plant 50% ethanol-water crude extracts


Retention time (min)

% of total area

Mass spectra

Assigned compounds

T triptera



51, 65, 91, 119, 120





53, 63, 69, 81, 97, 109, 126





60, 73, 83, 97, 115, 129, 143, 157, 171, 185, 199, 213, 227, 256

n-Hexadecanoic acid




57, 71, 107, 135, 320


D. winitii



51, 77, 107, 135, 150





65, 96, 111, 139, 154





111, 126, 141, 169, 184





77, 91, 124, 137, 180





60, 73, 83, 97, 115, 129, 143, 157, 171, 185, 199, 213, 227, 256

n-Hexadecanoic acid




57, 107, 135, 152, 320


A. harmandii



51, 77, 107, 135, 150





77, 91, 124, 137, 180





60, 73, 83, 97, 115, 129, 143, 157, 171, 185, 199, 213, 227, 256

Hexadecanoic acid




57, 74, 98, 112, 134, 239, 257, 299

Hexadecanoic acid, 2-hydroxy-1-(hydroxymethyl)ethyl ester)




43, 57, 74, 98, 112, 134, 154, 267, 284, 298, 327, 341, 358

Glyceryl monosterate

The GC chromatograms of the T. triptera, D. winitii, and A. harmandii extracts differed significantly. A GC peak of the retention time ranging from 23 to 24 min was found in the GC chromatograms of the three crude extracts, indicating that they may contain similar constituents. This peak region could not be identified by MS because the peaks were merged. The MS profiles of all of the crude extracts revealed that the crude extracts of the three plants had two identical compounds, namely vinylphenol and hexadecanoic acid, which are the most common phenolic and fatty acids in plants. Based on the identification of the extant phytochemicals in the 50% ethanol-water crude extracts using the MS database, the 50% ethanol-water crude extracts possessed the same GC retention time. However, the whole MS spectra of the individual 50% ethanol-water crude extracts appeared different, indicating the presence of different compounds.

This study is the first report of cell-based assays for the anticancer effects of selected plants. A. harmandii was considered to have the most potential for further study regarding its apoptosis-inducing mechanism, based on the findings of the flow cytometry analyses. Its bioactive constituents and anticancer activity toward other cancer cell types should be determined.


The 50% ethanol-water crude extracts of D. winitii, T. triptera, and A. harmandii showed anticancer activity in vitro.



Dulbecco’s modified Eagle’s medium




fetal bovine serum


gas chromatography/mass spectrometry


neutral red


phosphate-buffered saline


propidium iodide


selectivity index





This work was supported by Khon Kaen University through the Plant Genetics Conservation Project under the patronage of Her Royal Highness Princess Maha Chakri Sirindhorn (fiscal year 2011) (54122). AN was supported by a scholarship from the Graduate School, Khon Kaen University. The authors would like to thank the Bureau of The Royal Household for permission to conduct the research, Ms. Chantima Saoha and Ms. Cholpajsorn Junhom for technical assistance, and Mr. Bryan Roderick Hamman and Mrs. Janice Loewen-Hamman for assistance with the English-language presentation of the manuscript.

Authors’ Affiliations

Faculty of Pharmaceutical Sciences, Khon Kaen University
Center for Research and Development of Herbal Health Products (CRD-HHP), Faculty of Pharmaceutical Sciences, Khon Kaen University
Graduate School, Faculty of Pharmaceutical Sciences, Khon Kaen University
Center for Research and Development of Medical Diagnostic Laboratories (CMDL), Khon Kaen University
Faculty of Associated Medical Sciences, Khon Kaen University


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